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Iopi®

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8-3201Model Series 3

by IOPI Medical LLC

Identity

Trade Name
IOPI® EUDAMEDFDA UDI
Generic Name
Dynamometer force gauge FDA UDI
Device Name
IOPI (Iowa Oral Performance Instrument) EUDAMED
The IOPI® Trainer (Model 3.2) is used to increase the strength and endurance of the tongue and lip in patients with oral motor disorders, including dysphagia, dysarthria, and obstructive sleep apnea. The IOPI® Trainer is intended for clinical use and use by patients outside their therapy sessions under the direction of a healthcare professional. FDA UDI
Model / Reference
Series 3 EUDAMED
8-3201 EUDAMED
Model 3.2 FDA UDI
Description
The IOPI® Trainer (Model 3.2) is used to increase the strength and endurance of the tongue and lip in patients with oral motor disorders, including dysphagia, dysarthria, and obstructive sleep apnea. The IOPI® Trainer is intended for clinical use and use by patients outside their therapy sessions under the direction of a healthcare professional. FDA UDI

Identifiers

Catalog Number
8-3201 FDA UDI
Primary DI / UDI-DI
10810091040246 EUDAMEDFDA UDI
Basic UDI-DI
081009104IOPISeries3MX EUDAMED
Direct Marketing DI
10810091040246 EUDAMED
FDA Product Code
IKE FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Dynamometer force gauge FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
890.1615 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Iopi® by IOPI Medical LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
IOPI Medical LLC
EUDAMED SRN
US-MF-000035535
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 48b1e4eb-e337-4ab7-8d43-885669438ff7 61 fields · synced May 30, 2026
  • FDA UDI 995c0c4c-d7df-4c74-9c4c-46f2b60ac325 36 fields · synced May 30, 2026